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Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation (PWMQC)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01987245
First Posted: November 19, 2013
Last Update Posted: April 29, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Jun Xu, Peking Union Medical College Hospital
  Purpose
Cardiopulmonary resuscitation(CPR) is the key to success for high-quality early cardiopulmonary resuscitation, and its success in the restoration of spontaneous circulation (ROSC), therefore, monitoring the quality of cardiopulmonary resuscitation and early identification ROSC is very important. Now there is no an easy, non-invasive and real-time method to monitor the quality of CPR. In this study the investigators hypothesis the pulse oximeter waveform can real-time monitor the quality of CPR ,and feedback the quality of CPR to the physicians.

Condition
Cardiopulmonary Arrest Cardiopulmonary Resuscitation Return of Spontaneous Circulation Pulse Oximeter Plethysmographic Waveform

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Application Research of Plethysmographic Waveform in Quality Control Feedback System During Cardiopulmonary Resuscitation

Resource links provided by NLM:


Further study details as provided by Jun Xu, Peking Union Medical College Hospital:

Primary Outcome Measures:
  • survival rate [ Time Frame: 4 weeks ]

Enrollment: 617
Study Start Date: January 2014
Study Completion Date: March 2015
Primary Completion Date: March 2015 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
emergency room sample of multi-centers
Criteria

Inclusion Criteria:

  • cardiopulmonary arrest, without do-not-resuscitation(DNR) patients
  • After cardiac arrest, there is no more than 10 minutes until basic life support.
  • must be carried out advanced life support (tracheal intubation and end-tidal carbon dioxide monitoring)
  • comply with ethical requirements and signed informed consent

Exclusion Criteria:

  • DNR patients
  • rib fractures
  • hemorrhagic shock caused cardiac arrest
  • severe anemia, hemoglobin less than 7g/dl
  • tension pneumothorax without closed drainage
  • pulmonary embolism or pericardial tamponade caused cardiac arrest
  • onychomycosis
  • people who paint fingernails
  • clearly influential peripheral oximetry underlying diseases (such as Raynaud's phenomenon, vasculitis)
  • The study physicians believe there is any case is not suitable for inclusion.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01987245


Locations
China
PUMCH
Beijing, China
Sponsors and Collaborators
Jun Xu
  More Information

Responsible Party: Jun Xu, Emergency Department, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT01987245     History of Changes
Other Study ID Numbers: 2013S-512
2011-4001-04 ( Other Grant/Funding Number: CHRDS )
First Submitted: November 5, 2013
First Posted: November 19, 2013
Last Update Posted: April 29, 2015
Last Verified: April 2015

Additional relevant MeSH terms:
Heart Arrest
Heart Diseases
Cardiovascular Diseases


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